| Literature DB >> 28252243 |
Takanori Soya1, Hirotaka Mori1, Yongseok Hong2, Yun Hee Koo2, Dongho Kim2, Atsuhiro Osuka1.
Abstract
Internally 1,3-phenylene- and 2,5-thienylene-bridged [46]decaphyrins 2 and 3 have been synthesized. While 2 shows modest aromatic character derived from the global 46π-conjugated circuit, 3 displays larger aromatic character owing to the contribution of an (annuleno)annulene-type network consisting of two twisted Möbius aromatic thia[28]hexaphyrin segments in addition to the global 46π-network. Upon protonation, these [46]decaphyrins underwent large structural changes to acquire strong aromaticity. Protonated 3 has been revealed to take on a planar structure composed of fused two triangular thia[28]hexaphyrin segments.Entities:
Keywords: Möbius aromaticity; annulenoannulene; decaphyrin; expanded porphyrin; protonation
Year: 2017 PMID: 28252243 DOI: 10.1002/anie.201700607
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336